Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.226749289C= , CM000664.2:g.226749289C= | GRCh38 |
| NC_000002.11:g.227614005C= , CM000664.1:g.227614005C= | GRCh37 |
| NC_000002.10:g.227322249C= | NCBI36 |
| NG_015830.1:g.54502G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005544.3:c.*22-13039G= MANE Select | NP_005535.1:n.*22-13039G= |
| ENST00000305123.6:c.*22-13039G= MANE Select | ENSP00000304895.4:n.*22-13039G= |
| NM_005544.2:c.*22-13039G= | NP_005535.1:n.*22-13039G= |
| ENST00000305123.5:c.*22-13039G= | ENSP00000304895.4:n.*22-13039G= |